Device recall
Z-2251-2016: Best Theratronics cabinet x-ray systems intended for use in the irradiation of…
FDA device recall · Class II · BEST THERATRONICS LTD.
Key facts
| Recall number (Z-number) | Z-2251-2016 |
|---|---|
| Recall event | 74637 |
| Product | Best Theratronics cabinet x-ray systems intended for use in the irradiation of blood and blood products (packaged in transfusion bags) to inactivate T-lymphocytes for the prevention of Graft Versus Host Disease. |
| Product code | MOT |
| Recalling firm | BEST THERATRONICS LTD. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 1, 2017 |
| FEI number | 3006946288 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database